Canonical Allele Identifier: PA2827971881
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216182

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Arg2635Lys
CA337404
NM_001354898.2:c.7904G>A